JPS57146741A - Preparation of alpha-alkoxyvinyl carbonate ester - Google Patents
Preparation of alpha-alkoxyvinyl carbonate esterInfo
- Publication number
- JPS57146741A JPS57146741A JP56032834A JP3283481A JPS57146741A JP S57146741 A JPS57146741 A JP S57146741A JP 56032834 A JP56032834 A JP 56032834A JP 3283481 A JP3283481 A JP 3283481A JP S57146741 A JPS57146741 A JP S57146741A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- reacted
- group
- phosgene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE: To obtain the titled compound useful as a reagent for introducing a protecting group of an amino group, etc. easily in high yield, by reacting a reaction product obtained from the reaction of phosgene with pyridine with a bisalkoxycarbonylmercury and an alcohol, etc. one after the ether.
CONSTITUTION: Phosgene is reacted with pyridine in an unreactive solvent at -10W-20°C to give chlorocarbonylpyridinium chloride of formulaI, which is then reacted with a compound of the formula Hg(CH2COOR)2 (R is alkyl) at -10W-20°C to afford an α-alkoxyvinyloxycarbonylpyridinium chloride of formula II. The resultant reaction mixture is then reacted with an alcohol or phenol of the formula R1OH (R1 is alcoholic or phenolic residue) at -10W0°Cto give the aimed compound of formula III. The aimed compound of formula III (R1 is benzyl, tert-butyl or trithylsilylethyl group) which has not been easily prepared can be easily obtained. The compound is useful as a reagent for introducing the protecting group into the amino group.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56032834A JPS57146741A (en) | 1981-03-06 | 1981-03-06 | Preparation of alpha-alkoxyvinyl carbonate ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56032834A JPS57146741A (en) | 1981-03-06 | 1981-03-06 | Preparation of alpha-alkoxyvinyl carbonate ester |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57146741A true JPS57146741A (en) | 1982-09-10 |
JPS6351139B2 JPS6351139B2 (en) | 1988-10-13 |
Family
ID=12369843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56032834A Granted JPS57146741A (en) | 1981-03-06 | 1981-03-06 | Preparation of alpha-alkoxyvinyl carbonate ester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57146741A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5780628A (en) * | 1996-02-01 | 1998-07-14 | Sumitomo Chemical Company, Limited | Process for producing dioxoquinazolines |
-
1981
- 1981-03-06 JP JP56032834A patent/JPS57146741A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5780628A (en) * | 1996-02-01 | 1998-07-14 | Sumitomo Chemical Company, Limited | Process for producing dioxoquinazolines |
Also Published As
Publication number | Publication date |
---|---|
JPS6351139B2 (en) | 1988-10-13 |
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